A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610740



Internal ID16051463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18996430..19003973hg38UCSC Ensembl
Innerchr8:18853940..18861483hg19UCSC Ensembl
Innerchr8:18898220..18905763hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg387544
hg197544
hg187544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12048n54
Supporting Variantsnssv1156350, nssv1156349
SamplesHGDP00096, HGDP00650
Known GenesPSD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610740
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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